An optical nanoreporter of endolysosomal lipid accumulation reveals enduring effects of diet on hepatic macrophages in vivo.

TitleAn optical nanoreporter of endolysosomal lipid accumulation reveals enduring effects of diet on hepatic macrophages in vivo.
Publication TypeJournal Article
Year of Publication2018
AuthorsGalassi TV, Jena PV, Shah J, Ao G, Molitor E, Bram Y, Frankel A, Park J, Jessurun J, Ory DS, Haimovitz-Friedman A, Roxbury D, Mittal J, Zheng M, Schwartz RE, Heller DA
JournalSci Transl Med
Volume10
Issue461
Date Published2018 10 03
ISSN1946-6242
KeywordsAnimals, Cell Survival, Diet, Disease Models, Animal, Endosomes, Gene Expression Regulation, Lipid Metabolism, Lipoproteins, LDL, Liver, Lysosomal Storage Diseases, Lysosomes, Macrophages, Male, Mice, Inbred C57BL, Nanoparticles, Non-alcoholic Fatty Liver Disease, Optical Imaging, Tissue Distribution
Abstract

The abnormal accumulation of lipids within the endolysosomal lumen occurs in many conditions, including lysosomal storage disorders, atherosclerosis, nonalcoholic fatty liver disease (NAFLD), and drug-induced phospholipidosis. Current methods cannot monitor endolysosomal lipid content in vivo, hindering preclinical drug development and research into the mechanisms linking endolysosomal lipid accumulation to disease progression. We developed a single-walled carbon nanotube-based optical reporter that noninvasively measures endolysosomal lipid accumulation via bandgap modulation of its intrinsic near-infrared emission. The reporter detected lipid accumulation in Niemann-Pick disease, atherosclerosis, and NAFLD models in vivo. By applying the reporter to the study of NAFLD, we found that elevated lipid quantities in hepatic macrophages caused by a high-fat diet persist long after reverting to a normal diet. The reporter dynamically monitored endolysosomal lipid accumulation in vivo over time scales ranging from minutes to weeks, indicating its potential to accelerate preclinical research and drug development processes.

DOI10.1126/scitranslmed.aar2680
Alternate JournalSci Transl Med
PubMed ID30282694
PubMed Central IDPMC6543545
Grant ListDP2 HD075698 / HD / NICHD NIH HHS / United States
T32 CA062948 / CA / NCI NIH HHS / United States
P30 CA008748 / CA / NCI NIH HHS / United States
R01 HL067773 / HL / NHLBI NIH HHS / United States
K08 DK101754 / DK / NIDDK NIH HHS / United States
R01 NS081985 / NS / NINDS NIH HHS / United States
Related Faculty: 
Jose Jessurun, M.D.

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